Electrographic seizures and brain hyperoxia may be key etiological factors for postconcussive deficits

Haris Malik, Marshal D. Wolff, G. Campbell Teskey, Richelle Mychasiuk

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3 Citations (Scopus)


Repetitive mild traumatic brain injuries (RmTBIs) are increasingly recognized to have long-term neurological sequelae in a significant proportion of patients. Individuals that have had RmTBIs exhibit a variety of sensory, cognitive, or behavioral consequences that can negatively impact quality of life. Brain tissue oxygen levels (PO2) are normally maintained through exquisite regulation of blood supply to stay within the normoxic zone (18–30 mmHg in the rat hippocampus). However, during neurological events in which brain tissue oxygen levels leave the normoxic zone, neuronal dysfunction and behavioral deficits have been observed, and are frequently related to poorer prognoses. The oxygenation response in the brain after RmTBIs/repeated concussions has been poorly characterized, with most preliminary research limited to the neocortex. Furthermore, the mechanisms by which RmTBIs impact changes to brain oxygenation and vice versa remain to be determined. In the current study, we demonstrate that upon receiving RmTBIs, rats exhibit posttraumatic, electrographic seizures in the hippocampus, without behavioral (clinical) seizures, that are accompanied by a long-lasting period of hyperoxygenation. These electrographic seizures and the ensuing hyperoxic episodes are associated with deficits in working memory and motor coordination that were reversible through attenuation of the posttraumatic and postictal (postseizure) hyperoxia, via administration of a vasoconstricting agent, the calcium channel agonist Bay K8644. We propose that the posttraumatic period characterized by brain oxygenation levels well above the normoxic zone, may be the basis for some of the common symptoms associated with RmTBIs.

Original languageEnglish
Pages (from-to)727-737
Number of pages11
JournalJournal of Neurophysiology
Issue number3
Publication statusPublished - Sept 2022


  • Bay K8644
  • hippocampus
  • mild traumatic brain injury
  • postictal
  • vasculature

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